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1. |
Editorial |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 415-415
P. M. E. Lewis,
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ISSN:0030-4921
DOI:10.1002/mrc.1270220702
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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2. |
13C NMR spectra of tricyclo[4.2.1.02,5]nonanes and tetracyclo[5.4.1.02,6.08,11]dodecanes |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 416-418
Yasutaka Ishii,
Toshimitsu Noda,
Masakazu Kawahara,
Masaya Ogawa,
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摘要:
AbstractThe13C NMR spectra of tricyclo[4.2.1.02,5]nonanes and tetracyclo[5.4.1.02,6.08,11]dodecanes and their dimethyl derivatives were measured to demonstrate the four‐membered ring annelation effects on the bicyclo[2.2.1]heptane skeleton, and the steric δ‐syneffects of the methyl groups attached to the four‐membered ring on the bridge carbons in these s
ISSN:0030-4921
DOI:10.1002/mrc.1270220703
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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3. |
13C NMR investigations of phenol–triethylamine complexes: Influence of hydrogen bond interaction on the electronic structure of the aliphatic chain |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 419-423
Marek Ilczyszyn,
Zdzisław Latajka,
Henryk Ratajczak,
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摘要:
AbstractThe influence of hydrogen bond formation on13C chemical shifts at the α and β positions of triethylamine and tri‐n‐butylamine has been investigated by dipole moment measurements and CNDO/2 calculations. It has been shown that a hydrogen bridge dipole moment occurs during complexation. Moreover, the change observed in the C‐αC‐β bond dipole moment is proportional to the hydrogen bridge dipole moment, but is approximately 100 times smaller. This change has been related to differences between the13C chemical shifts at the α and β posi
ISSN:0030-4921
DOI:10.1002/mrc.1270220704
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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4. |
Compounds with bridgehead nitrogen. 48—stereochemistry of the 5‐methylperhydropyrido[3,2,1‐i,j][3,1]‐benzoxazines |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 424-427
Trevor A. Crabb,
Philip A. Jupp,
Christopher H. Turner,
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摘要:
AbstractSix of the eight possible diastereoisomeric 5‐methylperhydropyrido[3,2,1‐i,j][3,1]benzoxazines have been synthesized, and the utility of the C‐3 methylene proton NMR parameters [J(3ax3eq) and Δ3ax3eq] in the assignment of configurations has been demons
ISSN:0030-4921
DOI:10.1002/mrc.1270220705
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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5. |
Glucosidation shifts of allylic and benzylic alcohols in13C NMR spectroscopy |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 428-430
Isao Horibe,
Shujiro Seo,
Yohko Yoshimura,
Kazuo Tori,
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摘要:
AbstractThe13C FT NMR spectra of β‐D‐glucopyranosides (including their tetraacetates) of several secondary allylic and benzylic alcohols were compared with those of methyl β‐D‐glucopyranoside and the corresponding parent alcohols. The characeristic glucosidation shifts observed for these alcohols may be applicable to the determination of the absolute configuration of the hydroxy group in these
ISSN:0030-4921
DOI:10.1002/mrc.1270220706
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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6. |
1H and13C NMR studies of some germacrones and isogermacrones |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 431-433
S. D. Simova,
N. V. Bozhkova,
A. S. Orahovats,
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摘要:
AbstractThe1H and13C NMR spectra of thetrans,trans‐,cis,cis‐ andcis‐C‐3–C‐4,trans‐C‐7–C‐8‐germacrones and of thecis‐C‐2–C‐3,trans‐C‐7–C–8,trans‐C‐2–C‐3,cis‐C‐7–C‐8‐ andcis,cis‐isogermacrones are analysed. The last two isogermacrones are new compounds. The C‐2–C‐3 double bond in the previously described isogermacrone is found to be ofcisc
ISSN:0030-4921
DOI:10.1002/mrc.1270220707
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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7. |
Conformational study of methyl esters of some aliphaticerythro‐ andthreo‐dichlorocarboxylic acids |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 434-438
Maija Pitkänen,
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摘要:
AbstractThe average conformations of methyl esters of some aliphaticerythro‐ andthreo‐dichlorocarboxylic acids in dilute carbon tetrachloride solutions have been determined from the vicinal proton–proton coupling constants and1H NMR shifts. The13C shift differences between theerythroandthreoforms are compared and discussed with regard to the differences in the average conforma
ISSN:0030-4921
DOI:10.1002/mrc.1270220708
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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8. |
13C NMR spectra ofp‐ andm‐substituted phenylN‐methyl‐ and phenylN,N‐dimethyl‐carbamates |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 439-445
Chisako Yamagami,
Narao Takao,
Takaaki Nishioka,
Toshio Fujita,
Yoshito Takeuchi,
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摘要:
Abstract13C NMR spectra ofp‐ andm‐substituted phenylN‐methylcarbamates, phenylN,N‐dimethylcarbamates andp‐ andm‐substituted phenyl propionates were recorded, and theirpara13C SCS (substituent chemical shifts) were analysed by DSP (dual substituent parameters) and DSP‐NLR (non‐linear resonance) equations. It was found that the fixed substituent Y, OCONHCH3, OCON(CH3)2and OCOC2H5, were all mild in the sense that DSP analysis gave a good correlation, leaving little room for improvement by the DSP‐NLR treatment. Further, the three series of compounds gave similar ρIand ρRvalues (paraderivatives, 3.2–3.3 and 17.7–18.0;metaderivatives, 5.1–5.2 and 21.8–22.0). Examination of the corresponding analyses of similar compounds indicated that the ρIand ρRvalues and, hence, their ratio ρR/ρR= λ, depended primarily on the nature of the atom through which the fixed substituent Y (e.g. α‐C, α‐N and α‐O) was bonded to the aromatic ring when the Y substituents are mild. The extent of this tendency for compounds w
ISSN:0030-4921
DOI:10.1002/mrc.1270220709
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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9. |
A1H and13C NMR study of carminic acid |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 446-449
P. Schmitt,
H. Günther,
G. Hägele,
R. Stilke,
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摘要:
AbstractThe1H and13C NMR spectra of carminic acid were completely assigned, thus confirming its structure and the conformation of the glucose residue.
ISSN:0030-4921
DOI:10.1002/mrc.1270220710
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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10. |
The study of longifolene by two‐dimensional NMR spectroscopy |
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Organic Magnetic Resonance,
Volume 22,
Issue 7,
1984,
Page 450-453
P. Joseph‐Nathan,
R. L. Santillan,
P. Schmitt,
H. Günther,
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PDF (341KB)
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摘要:
AbstractThe complete assignment of the13C NMR spectrum of longifolene was achieved from double quantum coherence measurements, while combined evaluation of a1H13C heteronuclear chemical shift correlation diagram and a homonuclear1HJ‐resolved diagram provided all proton chemical shifts. Conformational information on the seven‐membered ring of the tricyclic sesquiterpene was obtained from proton chemical shift considera
ISSN:0030-4921
DOI:10.1002/mrc.1270220711
出版商:John Wiley&Sons Limited
年代:1984
数据来源: WILEY
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